Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs3890745
MMEL1
0.925 0.200 1 2622185 intron variant T/C snv 0.40 3
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 2
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 2
rs744877
CD160
0.882 0.200 1 145720709 intron variant C/A snv 0.47 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs10919563
PTPRC
0.925 0.120 1 198731313 intron variant G/A snv 0.21 1
rs1111695
PHTF1
1.000 0.120 1 113701277 intron variant C/A snv 0.65 1
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs11203366
PADI4
0.925 0.200 1 17331039 missense variant G/A snv 0.56 0.55 1
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 1